Fanconi anemia complementation group A

Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides instructions for making a protein that is involved in the Fanconi anemia (FA) pathway.

Also known as: FANCA, FANCA Fanconi anaemia, FANCA Fanconi anemia, Fanconi Anemia, complementation group type a, Fanconi anaemia caused by mutation in FANCA, Fanconi anaemia complementation group type A, Fanconi anemia caused by mutation in FANCA, Fanconi anemia complementation group A

115 clinical trials for this condition and its sub-types.